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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 1
2000 2
2003 1
2005 1
2006 1
2007 4
2008 1
2009 2
2010 1
2011 1
2012 7
2013 7
2014 11
2015 10
2016 4
2017 4
2018 5
2019 10
2020 15
2021 10
2022 12
2023 5

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103 results

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Page 1
Rezidivierende fulminante Myokarditis mit wiederholtem Einsatz der ECMO bei einem Kind.
Vercek G, Markelj G, Mlakar G, Primec ZR, Bertok S, Writzl K, Stefanija MA, Bajic S, Vesel S, Ihan A, Stritar A, Pokorn M, Kovac J, Debeljak M, Vidmar I, Avcin T, Grosek S. Vercek G, et al. Among authors: debeljak m. Klin Padiatr. 2019 Mar;231(2):80-86. doi: 10.1055/a-0831-2593. Epub 2019 Mar 14. Klin Padiatr. 2019. PMID: 30870874 German.
DNASE1L3 deficiency, new phenotypes, and evidence for a transient type I IFN signaling.
Tusseau M, Lovšin E, Samaille C, Pescarmona R, Mathieu AL, Maggio MC, Selmanović V, Debeljak M, Dachy A, Novljan G, Janin A, Januel L, Gibier JB, Chopin E, Rouvet I, Goncalves D, Fabien N, Rice GI, Lesca G, Labalme A, Romagnani P, Walzer T, Viel S, Perret M, Crow YJ, Avčin T, Cimaz R, Belot A. Tusseau M, et al. Among authors: debeljak m. J Clin Immunol. 2022 Aug;42(6):1310-1320. doi: 10.1007/s10875-022-01287-5. Epub 2022 Jun 7. J Clin Immunol. 2022. PMID: 35670985
Analytical Validation of SOD2 Genotyping.
Debeljak M, Riel S, Lin MT, Eshleman JR, Paller CJ. Debeljak M, et al. Methods Protoc. 2022 Dec 31;6(1):4. doi: 10.3390/mps6010004. Methods Protoc. 2022. PMID: 36648953 Free PMC article.
The Role of Epigenetic Modifications in Late Complications in Type 1 Diabetes.
Čugalj Kern B, Trebušak Podkrajšek K, Kovač J, Šket R, Jenko Bizjan B, Tesovnik T, Debeljak M, Battelino T, Bratina N. Čugalj Kern B, et al. Among authors: debeljak m. Genes (Basel). 2022 Apr 15;13(4):705. doi: 10.3390/genes13040705. Genes (Basel). 2022. PMID: 35456511 Free PMC article. Review.
Next-Generation Sequencing in Newborn Screening: A Review of Current State.
Remec ZI, Trebusak Podkrajsek K, Repic Lampret B, Kovac J, Groselj U, Tesovnik T, Battelino T, Debeljak M. Remec ZI, et al. Among authors: debeljak m. Front Genet. 2021 May 26;12:662254. doi: 10.3389/fgene.2021.662254. eCollection 2021. Front Genet. 2021. PMID: 34122514 Free PMC article. Review.
Integrative Transcriptomic Profiling of the Wilms Tumor.
Avčin SL, Črepinšek K, Jenko Bizjan B, Šket R, Kovač J, Vrhovšek B, Blazina J, Blatnik O, Kordič R, Kitanovski L, Jazbec J, Debeljak M, Tesovnik T. Avčin SL, et al. Among authors: debeljak m. Cancers (Basel). 2023 Jul 28;15(15):3846. doi: 10.3390/cancers15153846. Cancers (Basel). 2023. PMID: 37568662 Free PMC article.
Heterozygous NPR2 Variants in Idiopathic Short Stature.
Stavber L, Gaia MJ, Hovnik T, Jenko Bizjan B, Debeljak M, Kovač J, Omladič JŠ, Battelino T, Kotnik P, Dovč K. Stavber L, et al. Among authors: debeljak m. Genes (Basel). 2022 Jun 15;13(6):1065. doi: 10.3390/genes13061065. Genes (Basel). 2022. PMID: 35741827 Free PMC article.
Validation Strategy for Ultrasensitive Mutation Detection.
Debeljak M, Noë M, Riel SL, Haley LM, Norris AL, Anderson DA, Adams EM, Suenaga M, Beierl KF, Lin MT, Goggins MG, Gocke CD, Eshleman JR. Debeljak M, et al. Mol Diagn Ther. 2018 Oct;22(5):603-611. doi: 10.1007/s40291-018-0350-z. Mol Diagn Ther. 2018. PMID: 29974360
103 results